FERRUM PHOSPHORICUM

Manufacturer
Remedy Makers
Effective date
2010-03-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:02:14

Label at a glance#

ProductFERRUM PHOSPHORICUM
Active ingredientFERRUM PHOSPHORICUM
Label structure2 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Free from yeast, wheat, corn, and soy.
DIRECTIONS: Dissolve 3 or 4 pellets
in mouth or under tongue 3 times a day or as directed by a physician.
Children 2 years and older take 1/2
adult dose.
INDICATIONS: To be used according
to standard homeopathic indications
for self limiting conditions such as
those indicated on the front panel or as directed by a physician.
Warnings: *Use only if cap and
seal are unbroken. * Keep this and all medications out of reach of children.
* If symptoms persist for more then 3
days, consult your physician.
*As with any drug, if your are pregnant or nursing a baby, seek the advice of a
health professional before using this product.*Store tightly closed in a cool, dark place.
Made according to The Homeopathic Pharmacopoeia of the United States by: Remedy Makers, Pomona, CA 91768

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FERRUM PHOSPHORICUM 30CFERRUM PHOSPHORICUM 30C

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130310191190924GTIN-13: 0310191190924
EAN-13: 0310191190924
GTIN-12: 310191190924
UPC-A: 310191190924
GTIN storage (14 digits): 00310191190924
fd9f30e4-50f8-45a9-8b6d-012ea033b0de.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10191-1909-22019-10-21C16284748780-1956f9ecf-d1d0-621f-e053-dbdaa90a74adFERRUM PHOSPHORICUM 30C (Ferrosoferric Phosphate)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10191-1909-2FERRUM PHOSPHORICUM164 in 1 VIAL, GLASSPELLET1641

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10191-1909FERRUM PHOSPHORICUM (FERROSOFERRIC PHOSPHATE) PELLET [REMEDY MAKERS]1Legacy NDC, 1 package rows20100316_e3a12847-32ac-4893-82d1-b8d8776ab03b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
FERRUM PHOSPHORICUMACTIVE INGREDIENT91GQH8I5F71
FERRUM PHOSPHORICUMACTIVE MOIETY91GQH8I5F71

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10191-190910191-1909-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
FERRUM PHOSPHORICUM91GQH8I5F7ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
38e4050d-3ff6-4653-8508-c66f7fb8693ae3a12847-32ac-4893-82d1-b8d8776ab03b2010-03-16Exact identifier
spl id: 38e4050d-3ff6-4653-8508-c66f7fb8693a
spl set id: e3a12847-32ac-4893-82d1-b8d8776ab03b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.